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将μ免疫球蛋白基因导入小鼠种系:在淋巴细胞中的特异性表达及功能性抗体的合成。

Introduction of a mu immunoglobulin gene into the mouse germ line: specific expression in lymphoid cells and synthesis of functional antibody.

作者信息

Grosschedl R, Weaver D, Baltimore D, Costantini F

出版信息

Cell. 1984 Oct;38(3):647-58. doi: 10.1016/0092-8674(84)90259-9.

Abstract

A functionally rearranged mu heavy chain immunoglobulin (lg) gene was introduced into the germ line of mice. The mu gene encodes a polypeptide which, combined with lambda 1 light chains, shows a specificity for binding the hapten NP. Four transgenic mice harboring 20-140 copies of the foreign mu gene expressed the gene specifically in spleen, lymph node, and thymus at a high level. Purified surface lg-positive B cells, Lyt 2-positive mature T cells, and thymocytes transcribed the foreign mu gene at a similarly high level, suggesting that control of lg gene rearrangement might be the only mechanism that determines the specificity of heavy chain gene expression within the lymphoid cell lineage. No transcription of the foreign mu gene was detected in nonlymphoid tissues with the exception of the heart which expressed the gene at a low level. The transgenic mice had up to 400-fold elevated serum levels of NP binding antibody, which contained a heavy chain with the characteristics of the foreign mu gene. The serum levels of endogenous heavy and light chains in transgenic mice appeared to be the same as in normal mice.

摘要

将一个功能重排的μ重链免疫球蛋白(Ig)基因导入小鼠种系。μ基因编码一种多肽,该多肽与λ1轻链结合后,显示出对半抗原NP的结合特异性。四只携带20 - 140个外源μ基因拷贝的转基因小鼠在脾脏、淋巴结和胸腺中高水平特异性表达该基因。纯化的表面Ig阳性B细胞、Lyt 2阳性成熟T细胞和胸腺细胞以类似的高水平转录外源μ基因,这表明Ig基因重排的控制可能是决定淋巴样细胞系内重链基因表达特异性的唯一机制。除心脏低水平表达该基因外,在非淋巴组织中未检测到外源μ基因的转录。转基因小鼠血清中NP结合抗体水平升高达400倍,其中含有具有外源μ基因特征的重链。转基因小鼠内源性重链和轻链的血清水平似乎与正常小鼠相同。

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